Canonical Allele Identifier: CA403381054
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090670C>T (hg19) chr19:g.4090672C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090672C>T , CM000681.2:g.4090672C>T GRCh38
NC_000019.9:g.4090670C>T , CM000681.1:g.4090670C>T GRCh37
NC_000019.8:g.4041670C>T NCBI36
NG_007996.1:g.38457G>A , LRG_750:g.38457G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1568G>A
ENST00000688002.1:n.3280G>A
ENST00000688751.1:n.265G>A
ENST00000689792.1:n.1033G>A
ENST00000262948.10:c.1129G>A MANE Select ENSP00000262948.4:p.Val377Met
ENST00000262948.9:c.1129G>A ENSP00000262948.3:p.Val377Met
ENST00000394867.8:c.838G>A ENSP00000378336.1:p.Val280Met
ENST00000597263.5:n.314G>A
ENST00000599021.1:c.239G>A
ENST00000600584.5:n.2578G>A
ENST00000601786.5:n.1430G>A
NM_030662.3:c.1129G>A , LRG_750t1:c.1129G>A NP_109587.1:p.Val377Met
XM_006722799.2:c.850G>A XP_006722862.1:p.Val284Met
XM_011528133.1:c.559G>A XP_011526435.1:p.Val187Met
NM_030662.4:c.1129G>A MANE Select NP_109587.1:p.Val377Met
Search 100 bp 5'
Search 100 bp 3'